Clinical Research Coordinator I (CRC1) Flagstaff

Arizona Liver Health

Employer page

#Medical Records #Regulatory Compliance #Healthcare #Data Analysis #Patient Outreach #Clinical Research #GCP #Informed Consent #Clinical Trials

Quick overview

The coordinator is responsible for managing clinical research data, conducting study visits, and performing medical measurements like EKGs and vital signs. They also handle regulatory documentation, subject screening, and the coordination of study supplies and medical records.

Requirements summary

A high school diploma is required, while an associate or bachelor's degree is preferred. Candidates should ideally have at least one year of clinical research experience and proficiency with CTMS and EDC systems.

high schoolassociate degreebachelor degreeCommunicationOrganizational SkillsProblem SolvingPatient CareData EntryVital SignsGCPMedical Record ManagementEKGPatient SchedulingClinical Research CoordinationSpanish BilingualCTMSIATAEDC EntryAudit Research Trials

Job description

About Us

Arizona Liver Health (ALH) is dedicated to driving high standards of care and advancing medical innovation through leading clinical trials, ensuring patient safety and regulatory compliance, and generating high-quality clinical data. Our network of multiphase, multitherapeutic research, standard of care, and VEN Centers sites is staffed by skilled providers, research, clinic, pharmacy, and patient outreach professionals. ALH operates state-of-the-art facilities and programs to meet the evolving needs of clinical research and overall patient treatment.
Job
Summary: Arizona Liver Health/Arizona Clinical Trials is looking for qualified candidates for the Clinical Research Coordinator I position in Flagstaff.

Title

Clinical
Research
Coordinator
I (CRC1)
Compensation: $23.00 - $28.00 per hour, depending on experience and qualifications
Status:
Full-time, 40-hours,
Monday-Friday, 8am-5pm,
Non-exempt
Location: Flagstaff, AZ (onsite) Essential job functions/duties Reasonable accommodation may be made to enable individuals with disabilities to perform these essential functions. File documents in the binder (I.e., subject source, labs) Enter clinical research data into appropriate fields. Transfer data from paper formats via computer, recorders, or scanners EDC entry Review and edit data to ensure completeness and accuracy of information; follow up with subjects to resolve problems or clarify data collected. Answer Queries Serve as back up for pharmacy and lab Curate data directly from clinical research Analyze statistical and graphical Data. Conduct clinical research study visits when assigned. Audit research trials Prepare documents and charts for subject visits. Assist patients with surveys Perform vital signs, arthrometric measurements, transient elastography, and EKG’s Quality control research visits and informed consent before screening visit is over Confirm correct IP prior to dispensation File the signed copy in the subject binder Obtain and print procedural/imaging reports for review by the investigator Print labs and prepare for Investigator to review File lab results to subject binder or where required Ensure W-9 and medical release forms are signed by subjects annually Conduct clinical research study visits when assigned Audit research trials Prepare correspondence, documentation, or presentation materials on findings Assist with the management of study supplies and order resupply Perform miscellaneous job-related duties as assigned Request medical records prior to visit and print for filing as needed Plan, schedule, and confirm of subject research visits as needed Update CTMS as needed Maintain training as needed including but not limited to GCP, IATA, EDC, Protocol training, Delegation of Authority and others as required

Benefits

Dental Insurance
Paid Time Off
Health Insurance
Vision Insurance
Educational Assistance
401K With Company Match
Sick Time
Short Term Disability
Long Term Disability
Company Holidays
HSA Plans
Employer Contribution
Shared Company Vehicles

High School Diploma or GED required Associate Degree or Bachelors degree is preferred At least 1 year of clinical research experience as a clinical research coordinator and experience working in a medical center or private practice is strongly preferred Experience using
CTMS system and
EDC program
Knowledge,
Skills,
Abilities: Excellent communication and problem-solving skills Ability to work effectively with a lead study coordinator on multiple assignments, in a fast paced, multi-tasked environment, exercising sound judgment in setting priorities with a strong attention to detail Bilingual - Spanish preferred Vaccine trial experience preferred Demonstrated excellent organizational skills. Demonstrated experience working as part of a team. Relevant subject matter knowledge.
Travel requirements: Some interoffice travel may be required with use of company vehicle or mileage reimbursement
Benefits &
Perks: Health, Dental, Vision (with HSA plans and employer contribution) 2 weeks PTO 5 days Sick Time 7 Company holidays + 2 Half-days 401K with company match Short & Long Term Disability Educational Assistance Shared company vehicles for required travel EEO statement It is the policy of the Institute for Liver Health DBA Arizona Liver Health and Arizona Clinical Trials to provide equal employment opportunities without regard to race, color, religion, sex, national origin, age, disability, marital status, veteran status, sexual orientation, genetic information or any other protected characteristic under applicable law. This policy relates to all phases of employment, including, but not limited to, recruiting, employment, placement, promotion, transfer, demotion, reduction of workforce and termination, rates of pay or other forms of compensation, selection for training, the use of all facilities, and participation in all company-sponsored employee activities. Provisions in applicable laws providing for bona fide occupational qualifications, business necessity or age limitations will be adhered to by the company where appropriate.
Notice to
Staffing
Agencies: It is our policy that any and all contact with third party staffing or recruitment vendors come through our Talent Acquisition Team directly. We have an established and preferred network of contracted partners that we engage if and when we deem it necessary. We request that staffing agencies refrain from repeatedly contacting our hiring managers or employees directly. Unsolicited resumes, onsite solicitations, and inquiries will not be considered or responded to. Overly persistent and pushy inquires may also be blocked across our network as spam. Thank you for your understanding and cooperation.

Clinical Research Coordinator I (CRC1) Flagstaff

Clinical Research Coordinator I (CRC1) Flagstaff

Quick overview

Requirements summary

Job description

About Us

Title

Benefits

Education & Experience

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